rapid real time pcr platform Search Results


book series rapid cycle real-time pcr  (Verlag GmbH)
90
Verlag GmbH book series rapid cycle real-time pcr
Book Series Rapid Cycle Real Time Pcr, supplied by Verlag GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+real+time+pcr+platform/rapid+cycle+real+time+pcr+methods+and+applications/10__1373_slash_clinchem__2004__037721-119-6-14
Average 90 stars, based on 1 article reviews
book series rapid cycle real-time pcr - by Bioz Stars, 2026-09
90/100 stars
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influenza virus v8 rapid real-time rt-pcr detection kit  (Beijing Anheal Laboratories Company Ltd)
90
Beijing Anheal Laboratories Company Ltd influenza virus v8 rapid real-time rt-pcr detection kit
(A) Maximum-likelihood phylogenetic tree of hemagglutinin (HA) genomic segment of H3N2 CIVs. The phylogenetic tree of the HA gene was estimated using genetic distances calculated by maximum likelihood under the GTRGAMMA + I model. Viruses labeled with a red “*” were selected for subsequent experiments. Black, red, dark purple, and aqua blue to indicated H3N2 CIVs from China, America, Thailand, and South Korea, respectively. A, B, C, D, E, F and G represent different antigen groups of H3N2 CIVs respectively. A full detailed HA gene tree with the consistent topology is shown in (Scale bar is in units of nucleotide substitutions per site). (B) Prevalence of mammalian adaption markers among H3N2 CIVs. The sequences of H3N2 CIVs available in NCBI were analyzed comparing with avian and human <t>influenza</t> <t>A</t> viruses. Color indicates frequency of indicated substitutions in H3N2 CIVs for each indicated time period. (C) Antigenic map based on the HI assay data. Open squares and filled circles represent the positions of antisera and viruses, respectively. A k-means clustering algorithm identified clusters. Strains belonging to the same antigenic cluster are encircled with an oval. The vertical and horizontal axes both represent antigenic distance. The spacing between grid lines is 1 unit of antigenic distance, corresponding to a two-fold dilution of antiserum in the HI assay. Details of the HI assay data are shown in .
Influenza Virus V8 Rapid Real Time Rt Pcr Detection Kit, supplied by Beijing Anheal Laboratories Company Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+real+time+pcr+platform/influenza+a+virus+v8+rapid+real+time+rt+pcr+detection+kit/bio_rxiv__2022__10__10__511550-131-13-22
Average 90 stars, based on 1 article reviews
influenza virus v8 rapid real-time rt-pcr detection kit - by Bioz Stars, 2026-09
90/100 stars
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rapid and sensitive real-time pcr assays  (DIATHEVA Inc)
90
DIATHEVA Inc rapid and sensitive real-time pcr assays
(A) Maximum-likelihood phylogenetic tree of hemagglutinin (HA) genomic segment of H3N2 CIVs. The phylogenetic tree of the HA gene was estimated using genetic distances calculated by maximum likelihood under the GTRGAMMA + I model. Viruses labeled with a red “*” were selected for subsequent experiments. Black, red, dark purple, and aqua blue to indicated H3N2 CIVs from China, America, Thailand, and South Korea, respectively. A, B, C, D, E, F and G represent different antigen groups of H3N2 CIVs respectively. A full detailed HA gene tree with the consistent topology is shown in (Scale bar is in units of nucleotide substitutions per site). (B) Prevalence of mammalian adaption markers among H3N2 CIVs. The sequences of H3N2 CIVs available in NCBI were analyzed comparing with avian and human <t>influenza</t> <t>A</t> viruses. Color indicates frequency of indicated substitutions in H3N2 CIVs for each indicated time period. (C) Antigenic map based on the HI assay data. Open squares and filled circles represent the positions of antisera and viruses, respectively. A k-means clustering algorithm identified clusters. Strains belonging to the same antigenic cluster are encircled with an oval. The vertical and horizontal axes both represent antigenic distance. The spacing between grid lines is 1 unit of antigenic distance, corresponding to a two-fold dilution of antiserum in the HI assay. Details of the HI assay data are shown in .
Rapid And Sensitive Real Time Pcr Assays, supplied by DIATHEVA Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+real+time+pcr+platform/rapid+and+sensitive+real+time+pcr+assays/pm30453144-78-9-5
Average 90 stars, based on 1 article reviews
rapid and sensitive real-time pcr assays - by Bioz Stars, 2026-09
90/100 stars
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rapid real-time pcr assay for l. pneumophila  (BD Diagnostics)
90
BD Diagnostics rapid real-time pcr assay for l. pneumophila
(A) Maximum-likelihood phylogenetic tree of hemagglutinin (HA) genomic segment of H3N2 CIVs. The phylogenetic tree of the HA gene was estimated using genetic distances calculated by maximum likelihood under the GTRGAMMA + I model. Viruses labeled with a red “*” were selected for subsequent experiments. Black, red, dark purple, and aqua blue to indicated H3N2 CIVs from China, America, Thailand, and South Korea, respectively. A, B, C, D, E, F and G represent different antigen groups of H3N2 CIVs respectively. A full detailed HA gene tree with the consistent topology is shown in (Scale bar is in units of nucleotide substitutions per site). (B) Prevalence of mammalian adaption markers among H3N2 CIVs. The sequences of H3N2 CIVs available in NCBI were analyzed comparing with avian and human <t>influenza</t> <t>A</t> viruses. Color indicates frequency of indicated substitutions in H3N2 CIVs for each indicated time period. (C) Antigenic map based on the HI assay data. Open squares and filled circles represent the positions of antisera and viruses, respectively. A k-means clustering algorithm identified clusters. Strains belonging to the same antigenic cluster are encircled with an oval. The vertical and horizontal axes both represent antigenic distance. The spacing between grid lines is 1 unit of antigenic distance, corresponding to a two-fold dilution of antiserum in the HI assay. Details of the HI assay data are shown in .
Rapid Real Time Pcr Assay For L. Pneumophila, supplied by BD Diagnostics, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+real+time+pcr+platform/a+rapid+real+time+pcr+assay+for+l++pneumophila+is+now+commercially+available/pm16388431-125-25-33
Average 90 stars, based on 1 article reviews
rapid real-time pcr assay for l. pneumophila - by Bioz Stars, 2026-09
90/100 stars
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portable, rapid real-time pcr system  (Nagai Nori USA INC)
90
Nagai Nori USA INC portable, rapid real-time pcr system
(A) Maximum-likelihood phylogenetic tree of hemagglutinin (HA) genomic segment of H3N2 CIVs. The phylogenetic tree of the HA gene was estimated using genetic distances calculated by maximum likelihood under the GTRGAMMA + I model. Viruses labeled with a red “*” were selected for subsequent experiments. Black, red, dark purple, and aqua blue to indicated H3N2 CIVs from China, America, Thailand, and South Korea, respectively. A, B, C, D, E, F and G represent different antigen groups of H3N2 CIVs respectively. A full detailed HA gene tree with the consistent topology is shown in (Scale bar is in units of nucleotide substitutions per site). (B) Prevalence of mammalian adaption markers among H3N2 CIVs. The sequences of H3N2 CIVs available in NCBI were analyzed comparing with avian and human <t>influenza</t> <t>A</t> viruses. Color indicates frequency of indicated substitutions in H3N2 CIVs for each indicated time period. (C) Antigenic map based on the HI assay data. Open squares and filled circles represent the positions of antisera and viruses, respectively. A k-means clustering algorithm identified clusters. Strains belonging to the same antigenic cluster are encircled with an oval. The vertical and horizontal axes both represent antigenic distance. The spacing between grid lines is 1 unit of antigenic distance, corresponding to a two-fold dilution of antiserum in the HI assay. Details of the HI assay data are shown in .
Portable, Rapid Real Time Pcr System, supplied by Nagai Nori USA INC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+real+time+pcr+platform/portable++rapid+real+time+pcr+system/pm28475952-28-5-13
Average 90 stars, based on 1 article reviews
portable, rapid real-time pcr system - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier

Image Search Results


(A) Maximum-likelihood phylogenetic tree of hemagglutinin (HA) genomic segment of H3N2 CIVs. The phylogenetic tree of the HA gene was estimated using genetic distances calculated by maximum likelihood under the GTRGAMMA + I model. Viruses labeled with a red “*” were selected for subsequent experiments. Black, red, dark purple, and aqua blue to indicated H3N2 CIVs from China, America, Thailand, and South Korea, respectively. A, B, C, D, E, F and G represent different antigen groups of H3N2 CIVs respectively. A full detailed HA gene tree with the consistent topology is shown in (Scale bar is in units of nucleotide substitutions per site). (B) Prevalence of mammalian adaption markers among H3N2 CIVs. The sequences of H3N2 CIVs available in NCBI were analyzed comparing with avian and human influenza A viruses. Color indicates frequency of indicated substitutions in H3N2 CIVs for each indicated time period. (C) Antigenic map based on the HI assay data. Open squares and filled circles represent the positions of antisera and viruses, respectively. A k-means clustering algorithm identified clusters. Strains belonging to the same antigenic cluster are encircled with an oval. The vertical and horizontal axes both represent antigenic distance. The spacing between grid lines is 1 unit of antigenic distance, corresponding to a two-fold dilution of antiserum in the HI assay. Details of the HI assay data are shown in .

Journal: bioRxiv

Article Title: Increased public health threat of avian-origin H3N2 influenza virus during evolution in dogs

doi: 10.1101/2022.10.10.511550

Figure Lengend Snippet: (A) Maximum-likelihood phylogenetic tree of hemagglutinin (HA) genomic segment of H3N2 CIVs. The phylogenetic tree of the HA gene was estimated using genetic distances calculated by maximum likelihood under the GTRGAMMA + I model. Viruses labeled with a red “*” were selected for subsequent experiments. Black, red, dark purple, and aqua blue to indicated H3N2 CIVs from China, America, Thailand, and South Korea, respectively. A, B, C, D, E, F and G represent different antigen groups of H3N2 CIVs respectively. A full detailed HA gene tree with the consistent topology is shown in (Scale bar is in units of nucleotide substitutions per site). (B) Prevalence of mammalian adaption markers among H3N2 CIVs. The sequences of H3N2 CIVs available in NCBI were analyzed comparing with avian and human influenza A viruses. Color indicates frequency of indicated substitutions in H3N2 CIVs for each indicated time period. (C) Antigenic map based on the HI assay data. Open squares and filled circles represent the positions of antisera and viruses, respectively. A k-means clustering algorithm identified clusters. Strains belonging to the same antigenic cluster are encircled with an oval. The vertical and horizontal axes both represent antigenic distance. The spacing between grid lines is 1 unit of antigenic distance, corresponding to a two-fold dilution of antiserum in the HI assay. Details of the HI assay data are shown in .

Article Snippet: We amplified the matrix gene by real-time reverse transcription (RT) PCR using the Influenza A Virus V8 Rapid Real-Time RT-PCR Detection Kit (Beijing Anheal Laboratories Co. Ltd., http://anheal.company.weiku.com ), and isolated and identified virus isolates using methods described previously ( ).

Techniques: Labeling, HI Assay